Carbonylation of nitrobenzene to N-methyl phenylcarbamate catalyzed by palladium-phenanthroline complexes -: Bifunctional activation by anthranilic acid

被引：35

作者：

Gasperini, M

Ragaini, F

Cenini, S

Gallo, E

机构：

[1] CNR, Dipartimento Chim Inorgan Met & Analit, I-20133 Milan, Italy

[2] CNR, ISTM, I-20133 Milan, Italy

来源：

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL | 2003年 / 204卷

关键词：

nitrobenzene; carbonylation; palladium; urethanes; carboxylic acids; AROMATIC NITRO-COMPOUNDS; REDUCTIVE CARBONYLATION; PHENYL ISOCYANATE; NITROAROMATIC COMPOUNDS; CARBOXYLIC-ACID; LIGANDS; INTERMEDIATE; COCATALYST; URETHANES; DERIVATIVES;

D O I：

10.1016/S1381-1169(03)00289-9

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

The palladium-phenanthroline catalyzed carbonylation reaction of nitrobenzene to methyl phenylcarbamate is known to be accelerated by both the addition of aniline and a carboxylic acid. Here, we report that combining the acidic and amino function in the same molecule, 2-NH2C6H4COOH, anthranilic acid, an higher activity is observed with respect to the use of simple benzoic acid. The 4-amino isomer does not show the same increased activity. (C) 2003 Elsevier Science B.V. All rights reserved.

引用

页码：107 / 114

页数：8

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